Canonical Allele Identifier: CA1868278938
Gene: ALDOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425380_101425381delinsAC , CM000671.2:g.101425380_101425381delinsAC GRCh38
NC_000009.11:g.104187662_104187663delinsAC , CM000671.1:g.104187662_104187663delinsAC GRCh37
NC_000009.10:g.103227483_103227484delinsAC NCBI36
NG_012387.1:g.15400_15401delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000647789.2:c.799+72_799+73delinsGT MANE Select ENSP00000497767.1:n.799+72_799+73delinsGT...
ENST00000648064.1:c.799+72_799+73delinsGT ENSP00000497990.1:n.799+72_799+73delinsGT...
ENST00000648758.1:c.799+72_799+73delinsGT ENSP00000497731.1:n.799+72_799+73delinsGT...
ENST00000649902.1:c.799+72_799+73delinsGT ENSP00000497216.1:n.799+72_799+73delinsGT...
ENST00000374855.8:c.799+72_799+73delinsGT ENSP00000363988.4:n.799+72_799+73delinsGT...
ENST00000616752.1:c.799+72_799+73delinsGT ENSP00000481363.1:n.799+72_799+73delinsGT...
NM_000035.3:c.799+72_799+73delinsGT NP_000026.2:n.799+72_799+73delinsGT
NM_000035.4:c.799+72_799+73delinsGT MANE Select NP_000026.2:n.799+72_799+73delinsGT
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